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Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia
- Source :
- Gene (Amst.) 282 (2002): 87–94. doi:10.1016/S0378-1119(01)00846-0, info:cnr-pdr/source/autori:Nobile C, Hinzmann B, Scannapieco P, Siebert R, Zimbello R, Perez-Tur J, Sarafidou T, Moschonas NK, French L, Deloukas P, Ciccodicola A, Gesk S, Poza JJ, Lo Nigro C, Seri M, Schlegelberger B, Rosenthal A, Valle G, Lopez de Munain A, Tassinari CA, Michelucci R./titolo:Identification and characterization of a novel human brain-specific gene, homologous to S. Scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia./doi:10.1016%2FS0378-1119(01)00846-0/rivista:Gene (Amst.)/anno:2002/pagina_da:87/pagina_a:94/intervallo_pagine:87–94/volume:282
- Publication Year :
- 2002
-
Abstract
- We describe the structure, genomic organization, and some transcription features of a human brain-specific gene previously localized to the genomic region involved in temporal lobe epilepsy and spastic paraplegia on chromosome 10q24. The gene, which consists of six exons disseminated over 16 kb of genomic DNA, is highly homologous to the porcine tmp83.5 gene and encodes a putative transmembrane protein of 141 amino acids. Unlike its porcine homolog, from which two mRNAs with different 5'-sequences are transcribed, the human gene apparently encodes three mRNA species with 3'-untranslated regions of different sizes. Mutation analysis of its coding sequence in families affected with temporal lobe epilepsy or spastic paraplegia linked to 10q24 do not support the involvement of this gene in either diseases. (C) 2002 Elsevier Science B.V. All rights reserved.
- Subjects :
- Untranslated region
DNA, Complementary
Swine
Molecular Sequence Data
Gene Expression
Nerve Tissue Proteins
Biology
Exon
Transcription (biology)
Genetics
medicine
Coding region
Animals
Humans
Amino Acid Sequence
Gene
Genomic organization
Paraplegia
Base Sequence
Sequence Homology, Amino Acid
Chromosomes, Human, Pair 10
Brain
Chromosome Mapping
Membrane Proteins
General Medicine
Human brain
Exons
Sequence Analysis, DNA
Molecular biology
Introns
genomic DNA
medicine.anatomical_structure
Epilepsy, Temporal Lobe
Genes
Mutation
Sequence Alignment
Myelin Proteins
Subjects
Details
- ISSN :
- 03781119
- Volume :
- 282
- Issue :
- 1-2
- Database :
- OpenAIRE
- Journal :
- Gene
- Accession number :
- edsair.doi.dedup.....bc36ef0ca65eee4d82d0632ff46454e7
- Full Text :
- https://doi.org/10.1016/S0378-1119(01)00846-0